HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-piperidinecarboxylate → HCID 59553429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | HCID 59553352 | HCID 59553352 | — |
| Product | HCID 59553429 | HCID 59553429 | — |
Reaction Steps
Compound is prepared from N-[4-(2-chloroethoxy)-naphthalen-1-yl]-3-fluoro-5-piperidin-1-yl-benzamide and piperidine-4-carboxylic acid ethyl ester according to conditions described in general procedure N. 1H NMR 300 MHz (CDCl3) 8.31(dd, 1H, J=1.2 and 8.4 Hz), 7.88(s, 1H), 7.83(d, 1H, J=7.5 Hz), 7.73(d, 1H, J=8.1 Hz), 7.54(m, 2H), 7.31(s, 1H), 6.98(d, 1H, J=7.8 Hz), 6.84(d, 1H, J=8.4 Hz), 6.76(d, 1H, J=11.7 Hz), 4.31(t, 2H, J=5.7 Hz), 4.14(q, 2H, J=6.9 Hz), 3.28(m, 4H), 3.05(m, 2H), 2.97 (t, 2H, J=5.7 Hz), 2.24-2.32 (m, 3H), 1.64-1.97(m, 10H), 1.25(t, 3H, J=7.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114873B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-69d46098197544f3a2a0a632f0e5281c |
| Source note | uspto-grants-2012_02 |